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Construction of core-shell structured electrocatalysts with a thin noble metal shell is an effective strategy for lowering the usage of the noble metal and improving electrocatalytic properties because of the structure-induced geometric and electronic effects. Here, the synthesis of a novel core-shell structured nanocatalyst consisting of a thin amorphous Pd shell and a crystalline PdCu core and its significantly improved electrocatalytic properties for both formic acid oxidation and oxygen reduction reactions are shown. The electrocatalyst exhibits 4.1 times higher catalytic peak current density and better stability in the formic acid oxidation compared to both a PdCu nanoalloy catalyst and a Commercial Pd-C catalyst. An excellent electrocatalytic performance of the core-shell nanocatalyst is also observed in the oxygen reduction reaction. Computational calculation results reveal that tuning of the electronic state of Pd by the amorphous shell and the Cu in the PdCu core weaken the binding strength of surface Pd─O bonds, leading to a bond elongation to facilitate bond breaking. As a result, the electrocatalytic activity in both formic acid oxidation and oxygen reduction reactions is enhanced.
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http://dx.doi.org/10.1002/smll.202409404 | DOI Listing |
Chem Commun (Camb)
September 2025
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, 225002, PR China.
The MOF-derived Pd-CeO/NC catalyst exhibited enhanced formic acid electrooxidation activity due to interfacial electronic reconstruction, which downshifted the Pd d-band centre, thereby promoting the indirect oxidation of HCOOH and facilitating CO* oxidation.
View Article and Find Full Text PDFAnal Chim Acta
November 2025
Chemical and Veterinary Investigations Office Stuttgart, Schaflandstraße 3/2, 70736, Fellbach, Germany.
Background: Previous studies involving cleanup via conventional solid-phase extraction (SPE) materials to overcome matrix effects for the polar organophosphonate and -phosphinate pesticides glyphosate, glufosinate, ethephon, fosetyl, and their various metabolites often showed limitations due to the existence of various matrix compounds in plant commodities with similar polarity. To overcome existing drawbacks, we utilized the unique selectivity provided by metal oxides as SPE materials. These were exploited in a novel automated online SPE-LC-MS/MS method which allowed analyte-specific trapping in the presence of excessive amounts of matrix compounds as typically contained in extracts of the Quick Polar Pesticides (QuPPe) method.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
State Key Laboratory of Green Biomanufacturing, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.; Key Laboratory of Industrial Biocatalysis, Ministry of Education, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.; Ordos Laboratory, Inner
Currently, electrocatalytic conversion of carbon dioxide into higher-value compounds is a promising approach. However, developing a stable and efficient catalyst with high selectivity for specific products remains a major challenge. Herein, we constructed a bismuth-based metal-organic framework (Bi-MOF) as a catalyst for the catalytic production of formic acid from carbon dioxide, to which different ratios of tin metal elements were doped.
View Article and Find Full Text PDFJ Chromatogr A
September 2025
Agro-Food Technology and Quality Laboratory, Regional Center of Agricultural Research of Meknes, National Institute of Agricultural Research, Rabat, Morocco. Electronic address:
The composition of the injection solvent is a critical, yet often underestimated, parameter in liquid chromatography-tandem mass spectrometry (LC-MS/MS). This study systematically evaluates the influence of injection solvent on the analysis of 90 pesticides by comparing mixtures of acetonitrile (ACN) with water and buffered mobile phase A (5 mM ammonium formate, 0.1% formic acid) across various ratios (10/90 to 50/50, v/v).
View Article and Find Full Text PDFNano Lett
September 2025
School of Energy and Power Engineering, Key Laboratory of Ocean Energy Utilization and Energy Conservation of Ministry of Education, Dalian University of Technology, Dalian 116024, China.
The practical application of formic acid for large-scale hydrogen storage is constrained by its low H production rates. Conventional strategies rely on excessive chemical additives to accelerate the initial deprotonation step for efficient dehydrogenation. However, this approach is energy-consuming and compromises the intrinsic hydrogen storage density (53 g L) of formic acid.
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